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Palladium-Catalyzed Carbonylative Coupling Reactions of N,N-Bis(methanesulfonyl)amides through C-N Bond Cleavage

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dc.contributor.authorLim, Minkyung-
dc.contributor.authorKim, Hyeji-
dc.contributor.authorBan, Jaeyoung-
dc.contributor.authorSon, Junghan-
dc.contributor.authorLee, Jae Kyun-
dc.contributor.authorMin, Sun-Joon-
dc.contributor.authorLee, Sang Uck-
dc.contributor.authorRhee, Hakjune-
dc.date.accessioned2021-06-22T11:21:45Z-
dc.date.available2021-06-22T11:21:45Z-
dc.date.issued2018-11-
dc.identifier.issn1434-193X-
dc.identifier.issn1099-0690-
dc.identifier.urihttps://scholarworks.bwise.kr/erica/handle/2021.sw.erica/5131-
dc.description.abstractPalladium-catalyzed carbonylative coupling reactions of various N,N-bis(methanesulfonyl)amides with arylboronic acids through C-N bond cleavage were carried out. The reactions proceeded under mild conditions in a short period of time without any additives to afford a wide range of unsymmetrical aryl ketones in excellent yields. This is the first example of a carbonylative coupling reaction using N,N-bis(methanesulfonyl)amide as a coupling substrate.-
dc.format.extent8-
dc.language영어-
dc.language.isoENG-
dc.publisherJohn Wiley & Sons Ltd.-
dc.titlePalladium-Catalyzed Carbonylative Coupling Reactions of N,N-Bis(methanesulfonyl)amides through C-N Bond Cleavage-
dc.typeArticle-
dc.publisher.location독일-
dc.identifier.doi10.1002/ejoc.201801124-
dc.identifier.scopusid2-s2.0-85053794422-
dc.identifier.wosid000449649100012-
dc.identifier.bibliographicCitationEuropean Journal of Organic Chemistry, v.2018, no.41, pp 5717 - 5724-
dc.citation.titleEuropean Journal of Organic Chemistry-
dc.citation.volume2018-
dc.citation.number41-
dc.citation.startPage5717-
dc.citation.endPage5724-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.subject.keywordPlusFRIEDEL-CRAFTS ACYLATION-
dc.subject.keywordPlusELECTRONICALLY-ACTIVATED AMIDES-
dc.subject.keywordPlusACYL-TRANSFER REAGENTS-
dc.subject.keywordPlusSUZUKI-MIYAURA-
dc.subject.keywordPlusARYLBORONIC ACIDS-
dc.subject.keywordPlusCARBOXYLIC ANHYDRIDES-
dc.subject.keywordPlusKETONE SYNTHESIS-
dc.subject.keywordPlusDIARYL KETONES-
dc.subject.keywordPlusIONIC LIQUIDS-
dc.subject.keywordPlusARYL BROMIDES-
dc.subject.keywordAuthorSynthetic methods-
dc.subject.keywordAuthorPalladium-
dc.subject.keywordAuthorC-N bond cleavage-
dc.subject.keywordAuthorAmides-
dc.subject.keywordAuthorCross-coupling-
dc.identifier.urlhttps://chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/ejoc.201801124-
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